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GFAP expression of human Schwann cells in tissue culture. 1-gen-1992 D., Bianchini; I. D., Martini; Cadoni, Angela; Zicca, Antonio; Tabaton, Massimo; Schenone, Angelo; S., Anfosso; A. S., Akkad; Zaccheo, Damiano; Mancardi, GIOVANNI LUIGI
Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families. 1-gen-1992 Bellone, Emilia; Mandich, Paola; Mancardi, GIOVANNI LUIGI; Schenone, Angelo; Uccelli, Antonio; Abbruzzese, Michele; Sghirlanzoni, A; Pareyson, D; Ajmar, F.
Expression of common acute lymphoblastic leukemia antigen (CD 10) by myelinated fibers of the peripheral nervous system. 1-gen-1993 Cadoni, Angela; Mancardi, GIOVANNI LUIGI; D., Zaccheo; A., Nocera; S., Barocci; D., Bianchini; Schenone, Angelo; E., Capello; Zicca, Antonio
Impairment of central motor conduction in diabetic patients. 1-gen-1993 Abbruzzese, Giovanni; Schenone, Angelo; Scramuzza, G; Caponnetto, C; Gasparetto, B; Adezati, L; Abbruzzese, M; Viviani, GIORGIO LUCIANO
WERNICKE-KORSAKOFF ENCEPHALOPATHY FOLLOWING BILIOPANCREATIC DIVERSION 1-gen-1993 Primavera, Alberto; Brusa, G; Novello, P; Schenone, Angelo; Gianetta, Ezio; Marinari, G; Cuneo, S; Scopinaro, Nicola
The POEMS syndrome: report of six cases. 1-gen-1994 D., Pareyson; R., Marazzi; P., Confalonieri; Mancardi, GIOVANNI LUIGI; Schenone, Angelo; A., Sghirlanzoni
Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three cases 1-gen-1994 Schenone, Angelo; Abbruzzese, Michele; Uccelli, Antonio; Mandich, Paola; James, R.; Bellone, Emilia; Giunchedi, M.; Rolando, S.; Capello, E.; Mancardi, GIOVANNI LUIGI
17p11.2 duplication is a common finding in sporadic cases of charcot-marie-tooth type 1 1-gen-1994 Mancardi, G. L.; Uccelli, A.; Bellone, E.; Sghirlanzoni, A.; Mandich, P.; Pareyson, D.; Schenone, A.; Abbruzzese, M.; Ajmar, F.
Progressive sensory-motor polyneuropathy with tomaculous changes is associated to 17p11.2 deletion. 1-gen-1995 Mancardi, GIOVANNI LUIGI; Mandich, Paola; Nassani, S.; Schenone, Angelo; James, R.; Defferrari, R.; Bellone, Emilia; Giunchedi, M.; Ajmar, Franco; Abbruzzese, Michele
Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patients. 1-gen-1995 Mandich, Paola; R., James; S., Nassani; R., Defferrari; Bellone, Emilia; Mancardi, GIOVANNI LUIGI; Schenone, Angelo; Abbruzzese, Michele; M., Rocchi; Ajmar, Franco
Insulin-like growth factor-II as a paracrine growth factor in human neuroblastoma cells 1-gen-1995 Leventhal, P S; Randolph, A E; Vesbit, T E; Schenone, A; Windebank, A; Feldman, E L
Hereditary neuropathy with liability to pressure palsies and inherited brachial plexus neuropathy--two genetically distinct disorders 1-gen-1995 Windebank, A J; Schenone, A; Dewald, G W
Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfolding 1-gen-1995 James, R.; Bellone, Emilia; Nelis, E.; Mandich, Paola; Schenone, Angelo; Mancardi, GIOVANNI LUIGI; VAN BROECHKOVEN, C.; Abbruzzese, Michele; Ajmar, Franco
Expression of high- and low-affinity neurotrophin receptors on human transformed B lymphocytes. 1-gen-1996 Schenone, Angelo; Gill, Js; Zacharias, Da; Windebank, Aj
Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: a reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients. 1-gen-1996 Bellone, Emilia; Schenone, Angelo; Mancardi, GIOVANNI LUIGI; G. A., Nicholson; Abbruzzese, Michele; F., Ajmar; Mandich, Paola
De novo duplication in Charcot-Marie Tooth type 1A. 1-gen-1996 Mandich, Paola; Bellone, Emilia; Schenone, Angelo; Mancardi, GIOVANNI LUIGI; Abbruzzese, Michele; Ajmar, Franco
Advances in Charcot–Marie–Tooth Disease Research: Cellular Function of CMT-Related Proteins, Transgenic Animal Models, and Pathomechanisms 1-gen-1997 Hans W., Müller; Ueli, Suter; Christine Van, Broeckhoven; O., Haneman; E., Nelis; V., Timmerman; S., Sancho; L., Barrio; P., Bolhuis; R., Dermietzel; M., Frank; A., Gabreëls Festen; C., Gillen; N., Haites; G., Levi; E., Mariman; R., Martini; K., Nave; B., Rautenstrauss; M., Schachner; Schenone, Angelo; C., Schneider; M., Schröder; K., Willecke
Underexpression of messenger RNA for peripheral myelin protein 22 in hereditary neuropathy with liability to pressure palsies 1-gen-1997 Schenone, Angelo; Nobbio, Lucilla; Mandich, Paola; Bellone, Emilia; Abbruzzese, Michele; Ajmar, Franco; Mancardi, GIOVANNI LUIGI; Windebank, Aj
mRNA distribution in adult human brain of GRIN2B, a N-methyl-D-aspartate (NMDA) receptor subunit. 1-gen-1997 Schito, Am; Pizzuti, A; DI MARIA, Emilio; Schenone, Angelo; Ratti, A; Defferrari, R; Bellone, Emilia; Mancardi, GIOVANNI LUIGI; Ajmar, F; Mandich, Paola
Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies 1-gen-1997 Schenone, Angelo; Nobbio, L.; Caponetto, C.; Abbruzzese, Michele; Mandich, Paola; Bellone, Emilia; Ajmar, Franco; Gherardi, G.; Windebank, A. J.; Mancardi, GIOVANNI LUIGI
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